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Passive transport

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Transport that does not require energy
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Passive diffusion across acell membrane.
Diffusion (a form of passive transport) across the phospholipid bilayer, which is semipermeable, is demonstrated through simple and facilitated diffusion. Simple diffusion does not require energy, while small, non-polar molecules move from a high to a low solute concentration. Facilitated diffusion also does not require energy, yet it needs a protein channel to move large and polar molecules.

Passive transport is a type ofmembrane transport that does not requireenergy to move substances acrosscell membranes.[1][2] Instead of usingcellular energy, likeactive transport,[3] passive transport relies on thesecond law of thermodynamics to drive the movement of substances across cell membranes.[1][2][4] Fundamentally, substances followFick's first law, and move from an area of high concentration to an area of low concentration because this movement increases theentropy of the overallsystem.[4][5] The rate of passive transport depends on thepermeability of the cell membrane, which, in turn, depends on the organization and characteristics of the membranelipids andproteins.[citation needed] The four main kinds of passive transport are simplediffusion,facilitated diffusion,filtration, and/orosmosis.

Passive transport followsFick's first law.

Diffusion

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Main article:Diffusion
Passive diffusion on a cell membrane.

Diffusion is the net movement of material from an area of high concentration to an area with lower concentration. The difference of concentration between the two areas is often termed as theconcentration gradient, and diffusion will continue until this gradient has been eliminated. Since diffusion moves materials from an area of higher concentration to an area of lower concentration, it is described as moving solutes "down the concentration gradient" (compared withactive transport, which often moves material from area of low concentration to area of higher concentration, and therefore referred to as moving the material "against the concentration gradient"). However, in many cases (e.g. passive drug transport) the driving force of passive transport can not be simplified to the concentration gradient. If there are different solutions at the two sides of the membrane with different equilibrium solubility of the drug, the difference in the degree of saturation is the driving force of passive membrane transport.[6] It is also true for supersaturated solutions which are more and more important owing to the spreading of the application of amorphous solid dispersions for drugbioavailability enhancement.

Simple diffusion and osmosis are in some ways similar. Simple diffusion is the passive movement of solute from a high concentration to a lower concentration until the concentration of the solute is uniform throughout and reaches equilibrium. Osmosis is much like simple diffusion but it specifically describes the movement of water (not the solute) across a selectively permeable membrane until there is an equal concentration of water and solute on both sides of the membrane. Simple diffusion and osmosis are both forms of passive transport and require none of the cell'sATP energy.

Speed of diffusion

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For passive diffusion, the law of diffusion states that the mean squared displacement isr2=2dDt{\displaystyle \langle r^{2}\rangle =2dDt} withd being the number of dimensions andD thediffusion coefficient). So to diffuse a distance of aboutx{\displaystyle x} takes timex2/2dD{\displaystyle \sim x^{2}/2dD}, and the "average speed" is2dD/x{\displaystyle \sim 2dD/x}. This means that in the same physical environment, diffusion is fast when the distance is small, but less when the distance is large.

This can be seen in material transport within the cell. Prokaryotes typically have small bodies, allowing diffusion to suffice for material transport within the cell. Larger cells like eukaryotes would either have very low metabolic rate to accommodate the slowness of diffusion, or invest in complex cellular machinery to allow active transport within the cell, such askinesin walking alongmicrotubules.

Example of diffusion: gas exchange

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A biological example of diffusion is thegas exchange that occurs duringrespiration within the human body.[7] Upon inhalation,oxygen is brought into thelungs and quickly diffuses across the membrane ofalveoli and enters thecirculatory system by diffusing across the membrane of the pulmonarycapillaries.[8] Simultaneously,carbon dioxide moves in the opposite direction, diffusing across the membrane of the capillaries and entering into the alveoli, where it can be exhaled. The process of moving oxygen into the cells, and carbon dioxide out, occurs because of the concentration gradient of these substances, each moving away from their respective areas of higher concentration toward areas of lower concentration.[7][8]Cellular respiration is the cause of the low concentration of oxygen and high concentration of carbon dioxide within the blood which creates the concentration gradient. Because the gasses are small and uncharged, they are able to pass directly through thecell membrane without any special membrane proteins.[9] No energy is required because the movement of the gasses followsFick's first law and thesecond law of thermodynamics.

Facilitated diffusion

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Main article:Facilitated diffusion
Depiction of facilitated diffusion.

Facilitated diffusion, also called carrier-mediated osmosis, is the movement of molecules across the cell membrane via special transport proteins that are embedded in the plasma membrane by actively taking up or excluding ions[14]. Through facilitated diffusion, energy is not required in order for molecules to pass through the cell membrane.[1] Active transport ofprotons byH+ ATPases[10] altersmembrane potential allowing for facilitated passive transport of particular ions such as potassium[11] down their charge gradient through high affinity transporters and channels.

Example of facilitated diffusion: GLUT2

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An example offacilitated diffusion is whenglucose is absorbed into cells throughGlucose transporter 2 (GLUT2) in the human body.[12][13] There are many other types ofglucose transport proteins, some that dorequire energy, and are therefore not examples of passive transport.[13] Since glucose is a large molecule, it requires aspecific channel to facilitate its entry acrossplasma membranes and into cells.[13] When diffusing into a cell through GLUT2, the driving force that moves glucose into the cell is the concentration gradient.[12] The main difference betweensimple diffusion andfacilitated diffusion is that facilitated diffusion requires atransport protein to 'facilitate' or assist the substance through the membrane.[14] After a meal, the cell is signaled to move GLUT2 into membranes of the cells lining the intestines calledenterocytes.[12] With GLUT2 in place after a meal and the relative high concentration of glucose outside of these cells as compared to within them, the concentration gradient drives glucose across the cell membrane through GLUT2.[12][13]

Filtration

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Main articles:Filtration andUltrafiltration (renal)
Filtration.

Filtration is movement of water and solute molecules across the cell membrane due to hydrostaticpressure generated by thecardiovascular system. Depending on the size of the membrane pores, only solutes of a certain size may pass through it. For example, the membrane pores of theBowman's capsule in the kidneys are very small, and onlyalbumins, the smallest of the proteins, have any chance of being filtered through. On the other hand, the membrane pores ofliver cells are extremely large, but not forgetting cells are extremely small to allow a variety of solutes to pass through and be metabolized.

Osmosis

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Main articles:Osmosis andTonicity
Effect of osmosis on blood cells under different solutions.

Osmosis is the net movement of watermolecules across a selectively permeable membrane from an area of high water potential to an area of low water potential. A cell with a less negative water potential will draw in water, but this depends on other factors as well such as solute potential (pressure in the cell e.g. solute molecules) and pressure potential (external pressure e.g. cell wall). There are three types of Osmosis solutions: the isotonic solution, hypotonic solution, and hypertonic solution. Isotonic solution is when the extracellular solute concentration is balanced with the concentration inside the cell. In the Isotonic solution, the water molecules still move between the solutions, but the rates are the same from both directions, thus the water movement is balanced between the inside of the cell as well as the outside of the cell. A hypotonic solution is when the solute concentration outside the cell is lower than the concentration inside the cell. In hypotonic solutions, the watermoves into the cell, down its concentration gradient (from higher to lower water concentrations). That can cause the cell to swell. Cells that don't have a cell wall, such as animal cells, could burst in this solution. A hypertonic solution is when the solute concentration is higher (think of hyper - as high) than the concentration inside the cell. In hypertonic solution, the water willmove out, causing the cell to shrink.

See also

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References

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  1. ^abc"5.2 Passive Transport - Biology 2e | OpenStax".openstax.org. 28 March 2018. Retrieved2020-12-06.
  2. ^ab"5.2A: The Role of Passive Transport".Biology LibreTexts. 2018-07-10. Retrieved2020-12-06.
  3. ^"5.3 Active Transport - Biology 2e | OpenStax".openstax.org. 28 March 2018. Retrieved2020-12-06.
  4. ^abSkene, Keith R. (2015)."Life's a Gas: A Thermodynamic Theory of Biological Evolution".Entropy.17 (8):5522–5548.Bibcode:2015Entrp..17.5522S.doi:10.3390/e17085522.
  5. ^"12.7 Molecular Transport Phenomena: Diffusion, Osmosis, and Related Processes - College Physics for AP® Courses | OpenStax".openstax.org. 12 August 2015. Retrieved2020-12-06.
  6. ^Borbas, E.; et al. (2016). "Investigation and Mathematical Description of the Real Driving Force of Passive Transport of Drug Molecules from Supersaturated Solutions".Molecular Pharmaceutics.13 (11):3816–3826.doi:10.1021/acs.molpharmaceut.6b00613.PMID 27611057.
  7. ^abWagner, Peter D. (2015-01-01)."The physiological basis of pulmonary gas exchange: implications for clinical interpretation of arterial blood gases".European Respiratory Journal.45 (1):227–243.doi:10.1183/09031936.00039214.ISSN 0903-1936.PMID 25323225.
  8. ^ab"22.4 Gas Exchange - Anatomy and Physiology | OpenStax".openstax.org. 25 April 2013. Retrieved2020-12-06.
  9. ^"3.1 The Cell Membrane - Anatomy and Physiology | OpenStax".openstax.org. 25 April 2013. Retrieved2020-12-06.
  10. ^Palmgren, Michael G. (2001-01-01). "PLANT PLASMA MEMBRANE H+-ATPases: Powerhouses for Nutrient Uptake".Annual Review of Plant Physiology and Plant Molecular Biology.52 (1):817–845.doi:10.1146/annurev.arplant.52.1.817.PMID 11337417.
  11. ^Dreyer, Ingo; Uozumi, Nobuyuki (2011-11-01)."Potassium channels in plant cells".FEBS Journal.278 (22):4293–4303.doi:10.1111/j.1742-4658.2011.08371.x.ISSN 1742-4658.PMID 21955642.S2CID 12814450.
  12. ^abcdKellett, George L.; Brot-Laroche, Edith; Mace, Oliver J.; Leturque, Armelle (2008). "Sugar absorption in the intestine: the role of GLUT2".Annual Review of Nutrition.28:35–54.doi:10.1146/annurev.nutr.28.061807.155518.ISSN 0199-9885.PMID 18393659.
  13. ^abcdChen, Lihong; Tuo, Biguang; Dong, Hui (2016-01-14)."Regulation of Intestinal Glucose Absorption by Ion Channels and Transporters".Nutrients.8 (1): 43.doi:10.3390/nu8010043.ISSN 2072-6643.PMC 4728656.PMID 26784222.
  14. ^Cooper, Geoffrey M. (2000)."Transport of Small Molecules".The Cell: A Molecular Approach. 2nd Edition.
Mechanisms for chemical transport throughbiological membranes
Passive transport
Active transport
Cytosis
Endocytosis
Exocytosis
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